Hvac5 0506
Hvac5 0506
Presented by :
Deryck Smith Consulting Engineers
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The definition and need for validation of HVAC Systems A qualification approach for HVAC Systems Retrospective qualification Inspection of HVAC Systems Maintenance of HVAC Systems
Action of proving, in accordance with the principles of Good Manufacturing Practice, that any procedure, process, equipment, material, activity or system actually leads to the expected results.
A system must be qualified to operate in a validated process Equipment and systems are qualified
A process is validated
A number of systems make up a process
DQ IQ OQ PQ -
VMP GEP -
Design Qualification
Installation Qualification
Operational Qualification
Performance Qualification
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Qualification requires :
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2.
Collaboration of experts
Budget
3.
Planning
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Planning : Which systems are critical / non-critical ? (Risk assessment) Direct or indirect impact (ISPE) Which aspects of the system will be qualified ? Which aspects of the system will be handled under GEP ?
These decisions have implications on the extent, cost and time of the qualification process.
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Critical Components
A critical component within a system
where the operation, contact, data, control, alarm or failure will have a direct impact on the quality of the product. Eg. Supply air fan in an AHU, HEPA filters, HVAC control system.
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Non-critical Components
A non-critical component within a system
where the operation, contact, data, control, alarm or failure will have an indirect, or no impact on the quality of the product. Eg. Main facility chiller, Eskom high tension transformer on site.
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Functional Design
(ie. How as schematic) Design Development Detail Design (ie. How to make) Impact Assessment
Operational Qualification
IQ Test Plan
(inc.PDI)
Installation Qualification
Implementation
ISPE Baseline Guide Vol.5
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Functional Design
(ie. How as schematic) Design Development Detail Design (ie. How to make) Impact Assessment
(inc.FAT)
(inc.PDI)
Implementation
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Validation policy Organizational structure of validation activities Summary of facilities, systems, equipment and
processes to be validated Documentation format to be used for protocols and reports Planning and scheduling Change control References to existing documents
Ref : PIC/S Annex.15
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GMP requirements
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First step in the qualification of new HVAC systems. It documents the design of the system and will include :
Functional Specification.
b) Technical / Performance specification for equipment. c) Detailed Air Flow Schematics. d) Detailed layout drawing of the system.
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Design takes into account process and personnel flow (cross-contamination issues)
Design details materials of construction. Design details safety requirements. Full details of the intended construction prior to implementation. Details all equipment that must be ordered.
ISPE Baseline Guide Vol.5
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Check lists for components to be installed can be used. Items such as fans, fan motors, cooling and heating coils, filters, temperature and relative humidity sensors and differential pressure gauges can be included in check lists.
Duct and pipe pressure test reports.
Calibration of additionally used instruments. Initial cleaning records. Basic commissioning checks. Maintenance requirements. IQ process checks that the correct components are installed in the correct location. Materials of construction Spare parts Change controls
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Operational control / operation within established limits and tolerances can be demonstrated by any of the following :
Ability to maintain temperature, relative humidity and pressure set points. Ability to provide air of sufficient quality and quantity to ensure achievement of specified cleanroom conditions. Ability to maintain any critical parameters stated in the DQ consistently.
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Practical aspects of OQ :
IQ reports must be completed and signed off. OQ protocols to be written and approved prior to completion. Measurement reports are required to demonstrate achievement of critical parameters as detailed in DQ.
Eg: * Temperature measurement report * Humidity measurement report * Differential pressure measurement report * Air flow direction measurement report * Room particle count measurement report * All drawings etc. done in as-built status * All maintenance/ cleaning instructions available * All O & M staff to be trained to use and maintain the HVAC system.
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qualified substitutes or simulated product, that have been developed from knowledge of the process and facilities, systems or equipment. Test to include a condition or set of conditions encompassing upper and lower operating limits.
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achievement of critical parameters over time. ( under manufacturing conditions) PQ is ongoing. PQ and OQ tests are sometimes performed in conjunction with one another.
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PQ tests can consist of the following :Air flow direction tests Room pressure tests Room temperature monitoring Room relative humidity monitoring Room particle monitoring Microbiological monitoring
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Retrospective qualification
What happens when a detailed DQ, IQ and PQ
process has not been performed ? Evidence should be available (or prepared), to support and verify the operating parameters and limits for the critical variables of the operating equipment. Additionally, the calibration, cleaning, preventative maintenance, operating procedures and operator training procedures and records should be documented. ( PIC/S Annex 15) Basically only OQ and PQ is carried out.
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Check that the manufacturer has : A VMP and a multi-functional team for validation A planned approach with defined requirements Identified and described processes An analysis of the amount of validation work to perform
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Check that the manufacturer has : Selected methods & tools for validation Created protocols for execution of the work Performed DQ, IQ, OQ, PQ and documented the results Exerted change control
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Check that the manufacturer has : Authentic electronic records & signatures Operating & Maintenance Manuals As-built drawings of the ECS (HVAC System) Schematic layout of the ECS (NB) Maintenance schedules
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consisting of DQ, IQ, OQ and PQ. Expensive and time consuming Requires the manufacturer to assess which systems are critical and which are less critical. Used to demonstrate that the systems are under control.
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Airflow Measurement
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